Five novel mutations in the SCNN1A gene causing autosomal recessive pseudohypoaldosteronism type 1
Welzel, Maik, Akin, Leyla, Büscher, Anja, Güran, Tülay, P Hauffa, Berthold, Högler, Wolfgang, Leonards, Julia, Karges, Beate, Kentrup, Heiner, Kirel, Birgul, Senses, Emine Esin Yalinbas, Tekin, Neslihan, Holterhus, Paul-Martin, Riepe, Felix G
Published in European journal of endocrinology (01.05.2013)
Published in European journal of endocrinology (01.05.2013)
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